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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648312Generated: October 25, 2026

t-Butyl (8-amino-1,2,3,4-tetrahydro-3-quinolyl)carbamate → 5-((Phenylmethyl)methylamino)-5,6-dihydro-4H-imidazo(4,5,1-ij)quinolin-2(1H)-one

https://huagongshe.com/reaction/1648312

Reaction equation

Participants

RoleNameHCIDCharge
Reactantt-Butyl (8-amino-1,2,3,4-tetrahydro-3-quinolyl)carbamateHCID 19108500—
ReactantDiethyl ether methanolHCID 21864698—
Product5-((Phenylmethyl)methylamino)-5,6-dihydro-4H-imidazo(4,5,1-ij)quinolin-2(1H)-oneHCID 19919484—

Reaction Steps

This compound was prepared by following the procedure of Example 44 part B, but substituting 1,2,3,4-tetrahydro-N3 -methyl-N3 -(phenylmethyl)quinoline-3,8-diamine for t-butyl (8-amino-1,2,3,4-tetrahydro-3-quinolyl)carbamate. The bulk of the product was converted to the hydrochloride salt, mp 145°-149° C. from methanol/ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05436240
Source datasetuspto-grants-1995_07
ORD IDord-46b35582400e4af981ef697cf605d7e3
Source noteuspto-grants-1995_07